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ANIL MENDIRATTA, M.D.
M.D.
Neurology Physician
NPI: 1669534178IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
205581-1(NY)
CMS Specialties
PrimaryNEUROLOGY
Education
WAKE FOREST UNIVERSITY SCHOOL OF MEDICINE
Class of 1995
Research & Publications (11)
Neurophysiologic intraoperative monitoring of scoliosis surgery.
PMID 19279500·J Clin Neurophysiol·2009
6-review
Thermodynamic and kinetic studies of H atom transfer from HMo(CO)3(eta(5)-C5H5) to Mo(N[t-Bu]Ar)3 and (PhCN)Mo(N[t-Bu]Ar)3: direct insertion of benzonitrile into the Mo-H bond of HMo(N[t-Bu]Ar)3 forming (Ph(H)C=N)Mo(N[t-Bu]Ar)3.
PMID 18788794·Inorg Chem·2008
8-other
Thermodynamic, kinetic, and computational study of heavier chalcogen (S, Se, and Te) terminal multiple bonds to molybdenum, carbon, and phosphorus.
PMID 18260626·Inorg Chem·2008
8-other
Comparison of thermodynamic and kinetic aspects of oxidative addition of PhE-EPh (E = S, Se, Te) to Mo(CO)3(PR3)2, W(CO)3(PR3)2, and Mo(N[tBu]Ar)3 complexes. The role of oxidation state and ancillary ligands in metal complex induced chalcogenyl radical generation.
PMID 16881661·J Am Chem Soc·2006
4-observational
A diamagnetic dititanium(III) paddlewheel complex with no direct metal-metal bond.
PMID 16711677·Inorg Chem·2006
8-other
Benzonitrile extrusion from molybdenum(IV) ketimide complexes obtained via radical C-E (E = O, S, Se) bond formation: toward a new nitrogen atom transfer reaction.
PMID 16594725·J Am Chem Soc·2006
8-other
Heterobimetallic reductive cross-coupling of benzonitrile with carbon dioxide, pyridine, and benzophenone.
PMID 16212356·Inorg Chem·2005
8-other
Epilepsy and common comorbidities: improving the outpatient epilepsy encounter.
PMID 16120491·Epileptic Disord·2005
6-review
Synthesis of a four-coordinate titanium(IV) oxoanion via deprotonation and decarbonylation of complexed formate.
PMID 15997278·Chem Commun (Camb)·2005
8-other
Molybdenum chalcogenobenzimidato complexes: radical synthesis and nitrile extrusion via beta-EPh (E = S, Se, and Te) elimination.
PMID 14686837·Inorg Chem·2003
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 710 W 168TH ST
NEW YORK, NY 10032 - Phone
- (212) 305-1742
Quick Facts
- NPI
- 1669534178
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 31
- Publications
- 11
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